Nanominerals assemblages and hazardous elements assessment in phosphogypsum from an abandoned phosphate fertilizer industry

The present work investigates hazardous elements and nanomineralogical assemblages of phosphogypsum waste from an abandoned phosphate fertilizer industry located in Santa Catarina state (Brazil). Correlations between the chemical composition, nanominerals, and ultrafine particles are discussed. Multifaceted physical-geochemical study provided a careful understanding of the nanomineralogical assemblage of the phosphogypsum waste. The electron beam investigation revealed the presence of many hazardous elements in the ultrafine particles. Cr, Pb, Mn, Se, Sr, and Zr, among others, were found in individual ultrafine particles and nanominerals in all studied samples. Besides that, rare earth elements were found in different concentration ranges, being Ce, La, and Nd, the rare earth elements, found in the higher concentrations, above 900 mg kg−1. The data supplied by this article are important to characterize the phosphogypsum waste, assessing the potential hazard to the environment and human health, and also, provides information to enable the designing of alternatives to manage this waste

Simultaneous production of mesoporous biochar and palmitic acid by pyrolysis of brewing industry wastes

Pyrolysis of malt bagasse was carried out to obtain simultaneously a mesoporous biochar and an oil fraction rich in palmitic acid. The best result for biochar production was at 500 °C with holding time of 10 min. The yields of biochar and pyrolytic oil in this condition were, 29.7 and 33.9 wt%, respectively. The pyrolysis temperature and holding time influenced the yields of the products. An increase in pyrolysis temperature (from 500 to 700 °C) and holding time (from 10 to 50 min) caused a decrease in biochar yield, a reduction in the volatile matter content and an increase in the amount of ash. Additionally, in the range studied in this work, the increase of the pyrolysis temperature caused a decrease in the specific surface area and total pore volume of the biochar. Meanwhile, the biochar presented interesting functional groups and a mesoporous character, which can be a precursor to obtain adsorbents, or even, be used as adsorbent. The pyrolytic oil was composed of oxygenated aromatic compounds, the main fraction being palmitic acid (27.3%), which can be used in a number of applications, including biodiesel production. This work demonstrated that an available and problematic waste, malt bagasse, can be converted simultaneously into a mesoporous biochar and, into a pyrolytic oil rich in palmitic acid. Biochar and pyrolytic oil, in turn, are products of great value and can be applied in several fields

Treatment of effluents containing 2-chlorophenol by adsorption onto chemically and physically activated biochars

The application of adsorption using biochars for the remediation of effluents containing emerging contaminants, including chlorophenols, is a hotspot and trend development in the literature. This treatment is more interesting when using readily available wastes and at no cost, such as malt bagasse, for example. Here, the biochars were produced from malt bagasse, by physical and chemical activation (with CO2 and ZnCl2, respectively) and employed as adsorbents in the remediation of effluents containing 2-chlorophenol. Results revealed that the activated biochars have mesoporous structures and surface areas of 161 m² g-1 (CO2) and 545 m² g-1 (ZnCl2). For both activated biochars, adsorption of 2-chlorophenol was favored under acid conditions, with the highest adsorption capacities found using ZnCl2-activated biochar. The maximum adsorption capacity using ZnCl2-activated biochar was 150 mg g-1. The process was endothermic and spontaneous. ZnCl2-activated biochar exhibited an efficiency of 98% (using a dosage of 10 g L-1) in the treatment of industrial effluents containing 2-chlorophenol.La aplicación de la adsorción mediante biocarros para la remediación de efluentes que contienen contaminantes emergentes, incluidos los clorofenoles, es un punto crítico y un desarrollo de tendencia en la literatura. Este tratamiento es más interesante cuando se utilizan residuos fácilmente disponibles y sin costo, como el bagazo de malta, por ejemplo. Aquí, los biocarros se produjeron a partir de bagazo de malta, mediante activación física y química (con CO2 y ZnCl2, respectivamente) y se emplearon como adsorbentes en la remediación de efluentes que contienen 2-clorofenol. Los resultados revelaron que los biocarros activados tienen estructuras mesoporosas y áreas superficiales de 161 m² g-1 (CO2) y 545 m² g-1 (ZnCl2). Para ambos biocarros activados, la adsorción de 2-clorofenol se vio favorecida en condiciones ácidas, con las capacidades de adsorción más altas encontradas utilizando biocarbón activado con ZnCl2. La capacidad máxima de adsorción usando biocarbón activado con ZnCl2 fue de 150 mg g-1. El proceso fue endotérmico y espontáneo. El biocarbón activado con ZnCl2 exhibió una eficiencia del 98% (usando una dosis de 10 g L-1) en el tratamiento de efluentes industriales que contienen 2-clorofenol

Leaching of rare earth elements from phosphogypsum

High amounts of phosphogypsum (PG) are generated in the production of phosphoric acid. Previous literature demonstrates that obtaining rare earth elements (REE) from PG is a promising alternative to managing this waste. However, the reported leaching efficiencies are low in most cases, or drastic leaching conditions are required. Therefore, this work aimed to study the leaching conditions of REE from PG to obtain high leaching efficiency values. Initially, a 24 factorial experimental design investigated the factors that affect the conventional acid leaching of REE from PG (leaching acid (citric and sulfuric acid), solid/liquid ratio, acid concentration, and temperature). Better leaching efficiency values of the sum of all REE (62.0% and 89.7% for citric and sulfuric acid, respectively) were obtained using an acid concentration of 3 mol L−1, solid/liquid ratio of 1/20 g mL−1, and temperature of 80 °C. Subsequently, the experiments optimization, performed through a central composite rotational design, indicated that the maximum leaching efficiency was achieved using a sulfuric acid concentration of 2.9 mol L−1, solid/liquid ratio of 1.7/20 g mL−1, and 55 °C. Under these conditions, the leaching efficiency of the sum of all REE was 90.0%. Leaching kinetics results showed that the equilibrium was reached in about 20 min for most REE. The mechanism investigation suggested that surface chemical reaction and diffusion through the boundary layer controlled the leaching

Nickel-Aluminium layered double hydroxide as an efficient adsorbent to selectively recover praseodymium and samarium from phosphogypsum leachate

International audienceThis study aimed to synthesize a green powdered layered double hydroxide (LDH) based on nickel-aluminum (Ni–Al-LDH) to evaluate its efficiency in the removal of rare earth elements (REEs), Praseodymium (Pr3+) and Samarium (Sm3+), from synthetic effluents and real leachate using phosphogypsum as a secondary source of REEs. Several characterization techniques were employed to evaluate the physicochemical properties of Ni-Al-LDH adsorbent, such as specific surface area and porosity, functional surface groups and phases, and point of zero charge. The characterization results indicated that Ni-Al-LDH exhibited a typical layered structure confirming the successful synthesis. The effect of key adsorption variables, such as pH, contact time, initial concentration, and temperature, on the REEs adsorption was extensively studied in single-factor experiments separately. The kinetic and equilibrium adsorption data agreeably fitted the Avrami and Sips models, respectively. The maximum adsorption capacities for Pr3+ and Sm3+ adsorption were 18.13 and 15.68 mg g-1 at 298 K, respectively. The thermodynamic parameters (ΔH0, ΔS0, ΔG0) indicated that the adsorption was spontaneous, favorable, and exothermic for both Pr3+ and Sm3+. The interactions between Pr3+ and Sm3+ onto Ni-Al-LDH suggest that multiple adsorption mechanisms are involved, such as ion exchange, precipitation, chelation, and pore filling. Finally, the Ni-Al-LDH could selectively recover REEs, specially Pr3+ and Sm3+, from the real phosphogypsum leachate. It has been demonstrated that Ni-Al-LDH is a promising adsorbent material that could be used as an adsorbent for the recovery of REEs from synthetic and real effluents